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Evaluation of Rapid Assay (Tox A/B Quik Chek) for the Detection of Clostridium difficile Toxins A and B / 대한임상미생물학회지
Korean Journal of Clinical Microbiology ; : 112-116, 2008.
Article in Korean | WPRIM | ID: wpr-217983
ABSTRACT

BACKGROUND:

Toxin immunoassay is widely used for rapid diagnosis of Clostridium difficile-associated diarrhea. The aim of this study was to evaluate the performance of Tox A/B Quik Chek test (TECHLAB, Blacksburg, VA, USA) compared to toxigenic culture.

METHODS:

From September 2006 to August 2007, 959 stools were examined by Tox A/B Quik Chek test and toxigenic culture (C. difficile culture plus tcdB PCR using colonies obtained from culture).

RESULTS:

Compared to the results of toxigenic culture, the sensitivity and specificity of Tox A/B Quik Chek test were 47.5% and 97.5%, respectively.

CONCLUSION:

The sensitivity of Tox A/B Quik Chek test was not high, but the specificity was high. Although Tox A/B Quik Chek test alone is not sufficient to diagnose Clostridium difficile-associated diarrhea, it may aid rapid diagnosis, early treatment and prevention of nosocomial spread of the infection, if supplemented by C. difficile culture or tissue culture cytotoxin assay.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Bacterial Proteins / Bacterial Toxins / Boron Compounds / Immunoassay / Polymerase Chain Reaction / Clostridioides difficile / Immunoenzyme Techniques / Sensitivity and Specificity / Clostridium / Early Diagnosis Type of study: Diagnostic study / Screening study Language: Korean Journal: Korean Journal of Clinical Microbiology Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Bacterial Proteins / Bacterial Toxins / Boron Compounds / Immunoassay / Polymerase Chain Reaction / Clostridioides difficile / Immunoenzyme Techniques / Sensitivity and Specificity / Clostridium / Early Diagnosis Type of study: Diagnostic study / Screening study Language: Korean Journal: Korean Journal of Clinical Microbiology Year: 2008 Type: Article